A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115303



Internal ID21298569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57688020..57693829hg38UCSC Ensembl
Innerchr16:57721932..57727741hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385810
hg195810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv443n145
Supporting Variantsnssv14097829, nssv14099290
Samplessample230, sample370
Known GenesGPR97
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115303
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer